ライフサイエンスコーパス: mite

1 verse invertebrate groups such as the Acari (mites).

2 ature inverted-repeat transposable elements (MITEs).

3 Dermatophagoides farinae, an allergenic dust mite.

4 ear whether replication of DWV occurs in the mite.

5 matic sensitization to pollen and house dust mite.

6 line and after sensitization with house dust mite.

7 and sustainable solutions for V. destructor mites.

8 with high DWV levels but not in the passaged mites.

9 gic rhinitis and sensitization to house dust mites.

10 ed some benefits for experiments with spider mites.

11 gh dose of LPS before exposure to house dust mites.

12 irway inflammation in response to house dust mites.

13 and functionality compared to the classified MITEs.

14 inst staple food antigens but not house dust mites.

15 on the beetle in the presence and absence of mites.

16 stent fitness benefits of breeding alongside mites.

17 organs for chemical defense in most oribatid mites.

18 , while symbiotic bacteria prevailed in prey mites.

19 including rotifers, nematodes, insects, and mites.

20 t before, during, and after infestation with mites.

21 We show that mites: 1) cause beetles to reduce the antibacterial acti

22 used DNA metabarcoding data of 6,023 feather mites (a total of 2,225 OTU representative sequences) fr

23 This decrease significantly reduced the mites' ability to transmit DWV to honey bees.

24 Densities of mites (Acari), which include fungivores, detritivores an

25 two herbivorous mite species: the wheat curl mite (Aceria tosichella; Eriophyidae) and two-spotted sp

26 The tomato russet mite, Aculops lycopersici, is among the smallest animals

27 d increase in DWV load was observed in these mites after 2 days.

28 patients who received at least two relevant mite AIT prescriptions in two different successive seaso

29 -cell responses during 2 years of house dust mite AIT were compared between responder and nonresponde

30 Dust mite allergen exposure modifies the estimated effect of

31 In addition, we discuss of house dust mite allergen extracts as a prototypical complex extract

32 ed with FEV1 in children exposed to low dust mite allergen levels, but negatively associated with FEV

33 the mite-induced allergy and preparation of mite allergen vaccines.

34 Diverse factors contribute to house dust mite allergenicity through the activation of innate immu

35 ranscripts from peanut, soybean, sesame, and mite allergens contained a higher density of gaps than t

36 of filaggrin-deficient mice exposed to dust mite allergens for 8 weeks significantly suppressed tota

37 IgE specific for staple foods and house dust mite allergens in DOCK8-deficient patients and healthy c

38 receptor for conserved FABPs found in common mite allergens that initiate type 2 immunity at mucosal

39 h as asthma during environmental exposure to mite allergens, and therefore provide important insights

40 ownregulation in a mouse model of house dust mite allergic airway inflammation.

41 ial phage-display library constructed from a mite-allergic patient and expressed as two recombinant f

42 chnology using human B cells from house dust mite-allergic patients was used to identify four Der p 2

43 3-secreting Th cells were high in house dust mite-allergic patients.

44 House dust mite allergics showed IgE reactivity only to complete al

45 Since 2015, for patients with house dust mite allergies, we used a standardized house dust mite e

46 his study included 2350 patients receiving a mite allergoid and 64 740 control patients.

47 e good efficacy of subcutaneous AIT with HDM mite allergoid in the treatment of allergic rhinitis and

48 6 years of follow-up, patients treated with mite allergoid required significantly fewer AR and asthm

49 containing carbamylated monomeric house dust mite allergoids was to determine the most effective and

50 , and Prevention and Incidence of Asthma and Mite Allergy (PIAMA) (The Netherlands).

51 of current allergic rhinitis (AR) related to mite allergy and asthma were based on yearly interviews

52 The fluorescence profile in the guts of mites allowed to feed on these bees was very different f

53 s a multi-host species in which dispersal of mites among host species prevents species divergence.

54 novel anthropogenic habitats for insects and mites, analysing a combination of local-scale experiment

55 or prolonged studies of individual eriophyid mites and also provided some benefits for experiments wi

56 However, how plants perceive mites and how this perception is translated into changes

57 e a synergistic time-lag interaction between mites and neonicotinoids that resulted in significantly

58 as miniature inverted transposable elements (MITEs), and Helitrons.

59 alternata, Aspergillus fumigatus, house dust mite, and ovalbumin) for 4 wk.

60 ommon allergen used in treatment followed by mite, and two or more allergens were used in 85% patient

61 hSP-D) has been shown to suppress house dust mite- and Aspergillus fumigatus-induced allergic inflamm

62 High densities of mites are especially effective at promoting beetle repro

63 ing their roles in human diseases.IMPORTANCE Mites are important group of arthropods that are associa

64 Mites are notorious for being vectors transmitting infec

65 Even though these mites are potent vectors of viruses, the virus-insectici

66 ature inverted repeat transposable elements (MITEs) are prevalent in eukaryotic genomes.

67 e and fitness consequences for the beetle of mite-associated changes to the bacterial community on th

68 Exposure to mites at age 6 and 18 months was assessed by measuring D

69 abidopsis (Arabidopsis thaliana) upon spider mite attack that encodes a two-domain protein containing

70 lecular role in signaling following a spider mite attack.

71 iation of M. sellnicki with N. fulva, single mite attacks against E. ruidum did not result in host ki

72 undance of 14 species of medically important mites based on total RNA sequencing data sets generated

73 n m 1 and the minor allergens Der p 10 (dust mite), Bla g 7 (cockroach), and Ani s 3 (fish parasite)-

74 Transmission of mite-borne virus such as Deformed Wing Virus (DWV) was a

75 he diversity and evolution of RNA viruses in mites, but also a solid knowledge base for studying thei

76 , fire reduced the biomass of microfauna and mites, but had no impact on mesofauna or macrofauna.

77 ualism between burying beetles and P. carabi mites, but more work is needed to understand the functio

78 r traps potentiated the uptake of house dust mites by CD11b(+)Ly-6C(+) dendritic cells and type 2 all

79 engineered S. alvi can kill parasitic Varroa mites by triggering the mite RNAi response.

80 ligate blood feeding mite, the northern fowl mite can cause anaemia, slower growth, and decreased egg

81 However, it remains unclear whether or not mites carry viruses that might play a role in human infe

82 a population-based birth cohort we measured mite, cat, and dog allergen levels in dust samples colle

83 2-fold in pulmonary epithelium of house dust mite-challenged mice.

84 cate viral replication, was detected only in mites collected from pupae with high DWV levels but not

85 We show that mites compete with beetle larvae for food in the absence

86 We also found that Varroa mites contain honey bee mRNAs, consistent with the acqui

87 ients suffering from ocular discomfort (mean mite count 3.3 +/- 2.9 per patient).

88 The mean mite count per patient in this Austrian dry eye unit pop

89 , 80.7% of them were previously unclassified MITEs, demonstrating a different genomic distribution an

90 iature inverted-repeat transposable element (MITE)-derived small interfering RNA (siRNA) (here referr

91 asal doses of an extract from the house dust mite Dermatophagoides farinae (Df) sharply increased the

92 most important allergens from the house dust mite Dermatophagoides pteronyssinus Identification of hu

93 to perform TIR/TDR, interspersed-repeat, and MITE detection in several species, including Arabidopsis

94 sensitive than the existing inverted repeat/MITE detection tools based on numerical approaches (i.e.

95 The mite develops within the protective silk cocoon of an Ec

96 ork that underlies induced defence to spider mites, differentially expressed genes that encode transc

97 Highly infested weak colonies facilitate mite dispersal and disease transmission to stronger and

98 length P-elements relationship parallels the MITEs/DNA-transposase in plants and SINEs/LINEs in mamma

99 en and proinflammatory, the other house dust mite driven and chemokine dominant, with the former demo

100 otch deficiency in mice prevented house dust mite-driven eosinophilic airway inflammation and signifi

101 er, when blowflies breed on the carrion too, mites enhance beetle reproductive success by eating blow

102 promoted allergic TH responses to house dust mite exposure.

103 dy hypothesizes that standardized house dust mite extract (HDM group) was superior to non-standardize

104 eks to either saline, DEP, and/or house dust mite extract (HDM).

105 age fluid of mice challenged with house dust mite extract after oral administration (50 mg/kg, qd).

106 Mice were chronically exposed to house dust mite extract and then infected with influenza to resembl

107 allergies, we used a standardized house dust mite extract for subcutaneous immunotherapy, rather than

108 the initial dose of standardized house dust mite extract was 1 JAU or less.

109 Standardized house dust mite extract was more effective than non-standardized ho

110 House dust mite extract, Alternaria alternata extract, or rIL-33 wa

111 In rSCIT using standardized house dust mite extract, lowering the target dose at the end of the

112 ly, SAA1 interacted directly with allergenic mite FABPs (Der p 13 and Blo t 13).

113 The interaction between mite FABPs and SAA1 activated the SAA1-binding receptor,

114 Mites fed fat body survived longer and produced more egg

115 Mites fed hemolymph showed fitness metrics no different

116 report for the first time that tropilaelaps mites feed on both pre- and post-capped stages of honey

117 tight regulation of hormonal cross talk upon mite feeding.

118 formed Wing Virus (DWV) was also enhanced by mites feeding on early larval stages.

119 y Ectatomminae, and the first ant associated mite for which such a context dependent life-style shift

120 and a lower quality of meibum compared with mite-free patients.

121 in skin prick test reactivity to house dust mite from 7.0 +/- 1.3 to 2.7 +/- 0.5 mm (P = .001).

122 in seven of the 26 recognized species of the mite genus Macrodinychus (Machrodynichidae).

123 Herein, we report that mite group 13 allergens of the fatty acid-binding protei

124 transport inhibitor of complex I (MET-I) and mite growth inhibitor (MGI) acaricides on multiple T. ur

125 zed and challenged with high-dose house dust mite (>10 mug) or with low-dose house dust mite (<3 mug)

126 gene expression suggests that migrations of MITEs have no detectable effect on the expression level

127 mice were challenged with PBS or house dust mite (HDM) (Days 0, 7, 14-18) and exposed to room air or

128 ographic studies suggest that the house dust mite (HDM) allergen Der p 5 potentially interacts with h

129 early immunological responses to house dust mite (HDM) allergen in offspring challenged from 0 to 4

130 House dust mite (HDM) allergens are responsible for the most preval

131 led atopic asthma associated with house dust mite (HDM) allergy, relative to non-asthmatic control su

132 llergic CRS mouse model, based on house dust mite (HDM) and Staphylococcus aureus enterotoxin B (SEB)

133 were challenged over 3 weeks with house dust mite (HDM) antigen.

134 iates airway remodeling following house dust mite (HDM) challenge with decreases in mucus production,

135 IgG antibodies in extracts of the house dust mite (HDM) Dermatophagoides farinae, the Australian cock

136 In the house dust mite (HDM) Dermatophagoides pteronyssinus, Der p 1, 2, 5

137 of airborne allergens such as the house dust mite (HDM) effectively activates both innate and adaptiv

138 House dust mite (HDM) extract is a common trigger of asthma in huma

139 House dust mite (HDM) extract was used to induce allergic airway in

140 Cs challenged with IL-4/IL-13 and house dust mite (HDM) extract.

141 h prolonged i.n exposure to crude house dust mite (HDM) extract.

142 by ovalbumin (OVA) in mice and by house dust mite (HDM) in guinea pigs, as well as investigating the

143 Using a house dust mite (HDM) model of allergic asthma and parabiosis, we d

144 3E in airway angiogenesis using a house dust mite (HDM) murine model of allergic asthma.

145 y relevant aeroallergens, such as house dust mite (HDM) or Alternaria alternata, to induce experiment

146 during type 2 immune responses to house dust mite (HDM) or helminth infection and to identify mechani

147 s) in response to RSV, poly(I:C), house dust mite (HDM) or IL-33 using RT-qPCR, Luminex and live cell

148 and immunological response of SQ house dust mite (HDM) SLIT-tablet treatment in relation to body wei

149 Mice were exposed to house dust mite (HDM) to provoke Th2-mediated immune responses.

150 hallenged with ovalbumin (OVA) or house dust mite (HDM), and accessed for TH2 inflammation.

151 analyze the role of B cells in a house dust mite (HDM)-based murine asthma model.

152 House dust mite (HDM)-challenged Apoe(-/-) mice display enhanced ai

153 herapeutic efficacy of SAHM1 in a house dust mite (HDM)-driven asthma model.

154 s with AR and in a mouse model of house dust mite (HDM)-induced allergic asthma and whether it contri

155 1 in a preclinical mouse model of house dust mite (HDM)-induced allergic sensitization and allergic a

156 ed psoriasis-like inflammation, a house dust mite (HDM)-induced asthma-like allergic lung inflammatio

157 s by lung phagocytes might dampen house dust mite (HDM)-induced lung inflammation has not been shown.

158 udy, we employed a mouse model of house dust mite (HDM)-induced lung inflammation to explore the pote

159 OVA- and house dust mite (HDM)-induced murine asthma models were used in thi

160 timulatory effects of IL-1beta on house dust mite (HDM)-induced release of thymic stromal lymphopoiet

161 histosoma mansoni or the allergen house dust mite (HDM).

162 ated intranasal administration of house dust mite (HDM).

163 , transcriptome and microbiome of house dust mites (HDM) has shown that Staphylococcus aureus (S. aur

164 House dust mites (HDM) may serve as carriers of bacteria responsibl

165 lls, BEAS-2B, directly exposed to house dust mites (HDM) resulted in enhanced DNA damage, as measured

166 an allergoid in the treatment of house dust mites (HDM)-induced allergic rhinitis and/or asthma base

167 dically important mites including house dust mites (HDM).

168 House dust mites (HDMs) are among the most important allergen sourc

169 House dust mites (HDMs) are sources of an extensive repertoire of a

170 e that sensitization of mice with house-dust mites (HDMs) in the presence of low-dose lipopolysacchar

171 Allergic rhinitis induced by house dust mites (HDMs) is a highly prevalent but often underdiagno

172 ens, including those derived from house dust mites (HDMs).

173 ntries demonstrate sensitivity to house dust mites (HDMs).

174 ges in cucumber leaves in response to spider-mite herbivory and that of metabolites that are potentia

175 acin C content decreased during early spider-mite herbivory.

176 direct and indirect defences against spider-mite herbivory.

177 as one sustainable approach to reducing the mites' impact on honey bees.

178 dance with an asthma exacerbation to receive mite-impermeable (active group) or control (placebo grou

179 To evaluate the use of house dust mite-impermeable bedding and its impact on severe asthma

180 Using prolonged exposure to house dust mite in mice, we developed a mouse model of persistent a

181 When challenged with house dust mite in vivo, Gimap5-deficient mice displayed an exacerb

182 y was to determine the prevalence of Demodex mites in eyelashes of Austrian patients with ocular disc

183 The prevalence of Demodex mites in patients with ocular discomfort is high.

184 for soil, poultry litter, and nest dwelling mites in the Western Palearctic.

185 Mites in their reproductive phase were then fed a diet c

186 reening of RNA virome in medically important mites including house dust mites (HDM).

187 Here we used a murine model of house dust mite-induced (HDM-induced) allergic inflammation followe

188 House dust mite-induced airway inflammation was assessed by using a

189 TRPC1 intensifies house dust mite-induced airway remodeling by facilitating epithelia

190 in Th2-polarized settings such as house dust mite-induced allergic airway inflammation, the lack of I

191 e of hBD2 in a steroid-sensitive, house dust mite-induced allergic airways disease (AAD) model and a

192 ct of PKM2 on the pathogenesis of house dust mite-induced allergic airways disease in C57BL/6NJ mice.

193 herefore provide important insights into the mite-induced allergy and preparation of mite allergen va

194 cell assays and a mouse model of house dust mite-induced asthma, we compared IL-4 vs IL-13 vs IL-4Ra

195 ssessed in a mouse model of acute house dust mite-induced asthma.

196 ed, subjected to an ovalbumin- or house dust mite-induced experimental asthma protocol.

197 Blockade of Runx2 inhibited the house dust mite-induced goblet cell differentiation with a 75% redu

198 inhibited lung eosinophilia after house dust mite-induced inflammation.

199 in the setting of ovalbumin- and house dust mite-induced lung inflammation.

200 herapy stimulates progressive integration of mite-induced Th cell-associated Th2-, FOXP3/IL2-, inflam

201 Prior to immunotherapy, mite-induced Th-cell response networks involved multiple

202 as also determined before, during, and after mite infestation of hens using animal-based welfare metr

203 Associations of a mite infestation with individual dry eye and lid paramet

204 scriptome and metabolome as result of spider mite infestation with opposite consequences for direct a

205 reduction or when challenged by chronic fur mite infestation.

206 Tropilaelaps mite infestations resulted in 3.4- and 6-fold increases

207 , analyzing, and running bioassays involving mite-infested and control brood extracts from three hone

208 t-generation sequencing, we investigated how mites influence the bacterial communities on the carcass

209 9.67% of total non-rRNA transcriptome in one mite library.

210 Mite life-history (parasite or parasitoid) was context d

211 ature inverted-repeat transposable elements (MITEs), long terminal repeat (LTR) retrotransposons, and

212 t mite (>10 mug) or with low-dose house dust mite (<3 mug).

213 ng rat, mouse, cockroach, cat, dog, and dust mites, measured in dust samples collected from inner-cit

214 mporal dynamics of Tr1 cells in a house dust mite model of allergic airway inflammation.

215 In the house dust mite model, Tfr cells repress the production of IgE and

216 gic airway disease using a murine house dust mite model.

217 We used ovalbumin and house dust mite models of asthma.

218 rogate the role of T(FR) cells in house dust mite models.

219 se that transmission of DWV type A by Varroa mites occurs in a non-propagative manner.

220 ties (i.e., the assemblage consisting of all mites of different species collected from the same bird

221 rently sold for control of fleas, ticks, and mites on companion animals and poultry.

222 he types of injury inflicted by tropilaelaps mites on different stages of honey bees, the survival of

223 Finally, analysis of the impact of MITEs on gene expression suggests that migrations of MIT

224 ere investigated for the presence of Demodex mites on sampled eyelashes.

225 c mice were repeatedly exposed to house dust mite or Alternaria alternata three times a week for up t

226 ated intranasal administration of house dust mite or the fungal allergen Alternaria alternata.

227 However, the impact of mites or other ectoparasites on hen behaviour or welfare

228 ic treatment thresholds, suggesting that the mites or their vectored viruses are becoming more virule

229 e of the allergens: birch, grass, house dust mite, or cat.

230 We use experimental models of house dust mite- or ovalbumin-induced airway inflammation and influ

231 The northern fowl mite, Ornithonyssus sylviarum, is one of the most common

232 igh exposure to indoor allergens (house dust mites, pets, molds, etc), tobacco smoke, and other pollu

233 We show that mite populations from different host species represent a

234 eed to be developed to mitigate tropilaelaps mite problems.

235 21 and 5 allergens are homologous house dust mite proteins known as mid-tier allergens.

236 A total of 343485 MITE putative sequences, including canonical, diverse an

237 tly different between the microbiota of prey mites reared with and without N. cucumeris.

238 representing a recent example of host (i.e., mite)-related parallel evolution from dicistronic to mon

239 huge impact on public health, the virome of mites remains unknown.

240 ill parasitic Varroa mites by triggering the mite RNAi response.

241 ere are genomic features associated with the mite's minute size and lifestyle.

242 Asthma Guidelines (separated for house dust mite SCIT, SLIT tablets and SLIT drops; patient populati

243 ic rhinitis (AR) prescriptions in successive mite seasons.

244 c asthma via different methods of house dust mite sensitization and challenge.

245 We used a model of house dust mite sensitization to challenge wild-type, Bcl6(fl/fl) F

246 The increase in risk of mite sensitization with increasing Der p 1 exposure was

247 nal history of atopy, eczema, and house dust mite sensitization.

248 286 (mean age, 7.7 yr; male sex, 65.8%) were mite sensitized, and 284 were randomized (146 to the act

249 We randomized mite-sensitized children with asthma (ages 3-17 yr) afte

250 lial cells and dendritic cells of house dust mite-sensitized mice to dampen IFN-beta expression and p

251 Within the entire population of MITEs sequences, 80.7% of them were previously unclassif

252 ss (cassava mosaic disease and cassava green mite severity); quality (dry matter content and caroteno

253 Northern fowl mites significantly increased hen preening behaviour and

254 etle Nicrophorus vespilloides, an associated mite species Poecilochirus carabi and their common enemy

255 three different putative multi-host feather mite species Proctophyllodes macedo Vitzthum, 1922, Proc

256 This pattern was found in all the mite species, suggesting that each of these species is a

257 lture medium was tested with two herbivorous mite species: the wheat curl mite (Aceria tosichella; Er

258 ens (ie, grass, olive/ash pollen, house dust mites), specific IgE did not show marked differences bet

259 vo, loss of T(FR) cells increased house-dust-mite-specific IgE and lung inflammation.

260 nt with SQ (standardised quality) house dust mite sublingual tablet for 1 year resulted in a decrease

261 day (from 11% [placebo] to 5% [SQ house dust mite sublingual tablet]) and an increased probability of

262 ay (from 16% [placebo] to 34% [SQ house dust mite sublingual tablet]).

263 eared predators are fed with factitious prey mites such as Tyrophagus putrescentiae.

264 nkliniella occidentalis, but not against the mite Tetranychus urticae, when compared with sterilized

265 the generalist herbivore two-spotted spider mite (Tetranychus urticae).

266 ichella; Eriophyidae) and two-spotted spider mite (Tetranychus urticae; Tetranychidae).

267 mis sativus) genotypes to chelicerate spider mites (Tetranychus urticae) during the first 3 days of i

268 e and compare the complete RNA virome within mites that are relevant to human health and diseases.

269 iature inverted repeat transposable element (MITE) that contains two additional transposons and produ

270 As an obligate blood feeding mite, the northern fowl mite can cause anaemia, slower g

271 common enemy, and thereby induces a phoretic mite to become a protective mutualist.

272 In this study, we exposed Varroa mites to DWV type A via feeding on artificially infected

273 udy demonstrates the ability of tropilaelaps mites to inflict profound damage on A. mellifera hosts.

274 utative 5' cis-regulatory enhancer within an MITE transposon and the enhanced allelic expression of C

275 yl-CoA carboxylase (ACC) of pest insects and mites upon foliar application.

276 Neoseiulus cucumeris is a predatory mite used for biological control of arthropod pests.

277 have emerged from East Asian honey bees, the mite Varroa destructor and the microsporidian Nosema cer

278 era) colonies is challenged by the parasitic mite Varroa destructor and the numerous harmful pathogen

279 for honey bees challenged with the parasitic mite Varroa destructor associated to the Deformed Wing V

280 The parasitic mite Varroa destructor is the greatest single driver of

281 mellifera is challenged by the ectoparasitic mite Varroa destructor, and the numerous harmful pathoge

282 with an enhanced fertility of the parasitic mite Varroa destructor, as a possible consequence of a h

283 irus (DWV), transmitted by the ectoparasitic mite Varroa destructor, especially throughout the overwi

284 al spread of a new vector, the ectoparasitic mite Varroa destructor, has dramatically altered DWV epi

285 y Iflaviridae, together with its vector, the mite Varroa destructor, is likely the major threat to th

286 cticides and of the ubiquitous ectoparasitic mite Varroa destructor, no data exist to show synergisti

287 rsity following the arrival of the parasitic mite Varroa destructor, the key DWV vector, we found hig

288 ng virus (DWV), an RNA virus vectored by the mite Varroa destructor.

289 The parasitic mite, Varroa destructor, has shaken the beekeeping and p

290 Mite vectoring has resulted in the emergence of virulent

291 This specialist honeybee mite vectors deformed wing virus (DWV), an important re-

292 hogen pressure, primarily due to a parasitic mite/virus complex.

293 % of all available host pupae) more than one mite was involved and behaved as parasitoids, draining t

294 Infestation with mites was associated with the presence of significantly

295 to certain allergens (cockroach, mouse, dust mite) was significantly associated with enhanced cytokin

296 , parental hay fever, and higher exposure to mites were associated with a broader polymolecular IgE s

297 Demodex mites were identified in 40.2% of patients suffering fro

298 ng support for monophyletic Acari (ticks and mites), which when considered as a single group represen

299 tal bacteria were more abundant in predatory mites, while symbiotic bacteria prevailed in prey mites.

300 is the first association of a macrodinychid mite with a species of the subfamily Ectatomminae, and t